Canonical Allele Identifier: CA127195730
Gene: MIR3936HG HGNC NCBI

Linked Data

dbSNP Id: rs1042624242
gnomAD v3: 5-132369656-G-A
gnomAD v4: 5-132369656-G-A
MyVariant Identifiers: chr5:g.131705348G>A (hg19) chr5:g.132369656G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132369656G>A , CM000667.2:g.132369656G>A GRCh38
NC_000005.9:g.131705348G>A , CM000667.1:g.131705348G>A GRCh37
NC_000005.8:g.131733247G>A NCBI36
NG_008982.1:g.4948G>A
NG_008982.2:g.4953G>A

Transcript Alleles

HGVS Amino-acid Change
NR_110997.1:n.73+188C>T
Search 100 bp 5'
Search 100 bp 3'